Survival advantage from imatinib compared with the combination interferon-α plus cytarabine in chronic-phase chronic myelogenous leukemia:: historical comparison between two phase 3 trials

被引:164
作者
Roy, Lydia
Guilhot, Joelle
Krahnke, Tillmann
Guerci-Bresler, Agnes
Druker, Brian J.
Larson, Richard A.
O'Brien, Steve
So, Charlene
Massimini, Giorgio
Guilhot, Francois
机构
[1] CHU La Miletrie, Dept Oncol Hematol & Cell Therapy, EA 3805, F-86021 Poitiers, France
[2] CHU La Miletrie, Clin Res Ctr, F-86021 Poitiers, France
[3] Novartis Pharmaceut, Basel, Switzerland
[4] CHU Brabois, Dept Hematol, Vandoeuvre Les Nancy, France
[5] Oregon Hlth & Sci Univ, Inst Canc, Portland, OR 97201 USA
[6] Univ Chicago, Chicago, IL 60637 USA
[7] Newcastle Univ, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England
关键词
D O I
10.1182/blood-2006-02-001495
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
In the multinational IRIS study comparing imatinib with interferon plus cytarabine (IFN/Ara-C) in patients with newly diagnosed chronic-phase chronic myelogenous leukemia (CP CML), imatinib demonstrated significantly higher rates of complete cytogenetic responses (CCyRs) and improved progression-free survival (PFS). However, because of a high early crossover rate to imatinib, survival benefit was not assessable. Here, we report the result of a study comparing long-term outcome of patients included in 2 prospective randomized trials: 551 patients assigned to imatinib in the IRIS trial from 2000 to 2001 and 325 patients who received the combination IFN/Ara-C in the CML91 trial between 1991 and 1996 before imatinib was available. With a follow-up of 42 months for both groups of patients, estimated CCyR, survival free of transformation, and overall survival were significantly higher with imatinib compared with IFN/Ara-C (P < .001, P = .004, and P < .001, respectively). Improved overall survival was also confirmed within different Sokal prognostic risk groups. Of interest, among all patients who achieved major cytogenetic response or CCyR at 12 months, the survival rate was similar irrespective of their treatment. In conclusion, within the limitation of this historical comparison, there is a survival advantage from first-line therapy with imatinib over IFN/Ara-C.
引用
收藏
页码:1478 / 1484
页数:7
相关论文
共 27 条
  • [1] Imatinib and pegylated human recombinant interferon-α2b in early chronic-phase chronic myeloid leukemia
    Baccarani, M
    Martinelli, G
    Rosti, G
    Trabacchi, E
    Testoni, N
    Bassi, S
    Amabile, M
    Soverini, S
    Castagnetti, F
    Cilloni, D
    Izzo, B
    de Vivo, A
    Messa, E
    Bonifazi, F
    Poerio, A
    Luatti, S
    Giugliano, E
    Alberti, D
    Fincato, G
    Russo, D
    Pane, F
    Saglio, G
    [J]. BLOOD, 2004, 104 (13) : 4245 - 4251
  • [2] A randomized study of interferon-α versus interferon-α and low-dose arabinosyl cytosine in chronic myeloid leukemia
    Baccarani, M
    Rosti, G
    de Vivo, A
    Bonifazi, F
    Russo, D
    Martinelli, G
    Testoni, N
    Amabile, M
    Fiacchini, M
    Montefusco, E
    Saglio, G
    Tura, S
    [J]. BLOOD, 2002, 99 (05) : 1527 - 1535
  • [3] Chronic myeloid leukemia and interferon-α:: a study of complete cytogenetic responders
    Bonifazi, F
    de Vivo, A
    Rosti, G
    Guilhot, F
    Guilhot, J
    Trabacchi, E
    Hehlmann, R
    Hochhaus, A
    Shepherd, PCA
    Steegmann, JL
    Kluin-Nelemans, HC
    Thaler, J
    Simonsson, B
    Louwagie, A
    Reiffers, J
    Mahon, FX
    Montefusco, E
    Alimena, G
    Hasford, J
    Richards, S
    Saglio, G
    Testoni, N
    Martinelli, G
    Tura, S
    Baccarani, M
    [J]. BLOOD, 2001, 98 (10) : 3074 - 3081
  • [4] COX DR, 1972, J R STAT SOC B, V34, P187
  • [5] The tyrosine kinase inhibitor CGP57148B selectively inhibits the growth of BCR-ABL-positive cells
    Deininger, MWN
    Goldman, JM
    Lydon, N
    Melo, JV
    [J]. BLOOD, 1997, 90 (09) : 3691 - 3698
  • [6] Efficacy and safety of a specific inhibitor of the BCR-ABL tyrosine kinase in chronic myeloid leukemia.
    Druker, BJ
    Talpaz, M
    Resta, DJ
    Peng, B
    Buchdunger, E
    Ford, JM
    Lydon, NB
    Kantarjian, H
    Capdeville, R
    Ohno-Jones, S
    Sawyers, CL
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2001, 344 (14) : 1031 - 1037
  • [7] Chronic myelogenous leukemia: Biology and therapy
    Faderl, S
    Talpaz, M
    Estrov, Z
    Kantarjian, HM
    [J]. ANNALS OF INTERNAL MEDICINE, 1999, 131 (03) : 207 - 219
  • [8] Results of a prospective phase 2 study combining imatinib, mesylate and cytarabine for the treatment of Philadelphia-positive patients with chronic myelogenous leukemia in chronic phase
    Gardembas, M
    Rousselot, P
    Tulliez, M
    Vigier, M
    Buzyn, A
    Rigal-Huguet, F
    Legros, L
    Michallet, M
    Berthou, C
    Cheron, N
    Maloisel, F
    Mahon, FX
    Facon, T
    Berthaud, P
    Guilhot, J
    Guilhot, F
    [J]. BLOOD, 2003, 102 (13) : 4298 - 4305
  • [9] Interferon alfa-2b combined with cytarabine versus interferon alone in chronic myelogenous leukemia
    Guilhot, F
    Chastang, C
    Michallet, M
    Guerci, A
    Harousseau, JL
    Maloisel, F
    Bouabdallah, R
    Guyotat, D
    Cheron, N
    Nicolini, F
    Abgrall, JF
    Tanzer, J
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1997, 337 (04) : 223 - 229
  • [10] CYTOGENETIC REMISSIONS IN CHRONIC MYELOGENOUS LEUKEMIA USING INTERFERON ALPHA-2A AND HYDROXYUREA WITH OR WITHOUT LOW-DOSE CYTOSINE-ARABINOSIDE
    GUILHOT, F
    DREYFUS, B
    BRIZARD, A
    HURET, JL
    TANZER, J
    [J]. LEUKEMIA & LYMPHOMA, 1991, 4 (01) : 49 - 55